Hair follicle dermal condensation forms via Fgf20 primed cell cycle exit, cell motility, and aggregation

Elife. 2018 Jul 31:7:e36468. doi: 10.7554/eLife.36468.

Abstract

Mesenchymal condensation is a critical step in organogenesis, yet the underlying molecular and cellular mechanisms remain poorly understood. The hair follicle dermal condensate is the precursor to the permanent mesenchymal unit of the hair follicle, the dermal papilla, which regulates hair cycling throughout life and bears hair inductive potential. Dermal condensate morphogenesis depends on epithelial Fibroblast Growth Factor 20 (Fgf20). Here, we combine mouse models with 3D and 4D microscopy to demonstrate that dermal condensates form de novo and via directional migration. We identify cell cycle exit and cell shape changes as early hallmarks of dermal condensate morphogenesis and find that Fgf20 primes these cellular behaviors and enhances cell motility and condensation. RNAseq profiling of immediate Fgf20 targets revealed induction of a subset of dermal condensate marker genes. Collectively, these data indicate that dermal condensation occurs via directed cell movement and that Fgf20 orchestrates the early cellular and molecular events.

Keywords: Fgf20; RNAseq; cell biology; dermal condensate; developmental biology; hair follicle; live imaging; mouse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Cell Aggregation
  • Cell Cycle*
  • Cell Lineage
  • Cell Movement*
  • Cell Shape
  • Dermis / cytology*
  • Dermis / ultrastructure
  • Fibroblast Growth Factor 9 / pharmacology
  • Fibroblast Growth Factors / metabolism*
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Hair Follicle / cytology*
  • Mice, Inbred C57BL
  • Morphogenesis
  • Receptors, Fibroblast Growth Factor / metabolism
  • Receptors, Vascular Endothelial Growth Factor / metabolism
  • SOXB1 Transcription Factors / metabolism
  • Signal Transduction
  • Transcription, Genetic

Substances

  • Actins
  • Fgf20 protein, mouse
  • Fibroblast Growth Factor 9
  • Receptors, Fibroblast Growth Factor
  • SOXB1 Transcription Factors
  • Fibroblast Growth Factors
  • Receptors, Vascular Endothelial Growth Factor

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.